@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I130_head
{
this:
np:hasAssertion
dgn-np:NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I130_assertion
a
np:Assertion
.
dgn-np:NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I130_provenance
a
np:Provenance
.
dgn-np:NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:6041
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN63bdb61c357c768f1235ec804cdc08a6
sio:SIO_000628
miriam-gene:6041
,
lld:C0009402
;
a
sio:SIO_001122
.
}
dgn-np:NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I130_provenance
{
dgn-np:NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I130_assertion
dcterms:description
"[We have previously reported that the common, functionally different variants Arg72Pro in p53 and Arg462Gln in RNASEL are associated with the age of disease onset of colorectal cancer in Lynch syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:17224235
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP588910.RAsYGaLjR7us-4XXq2U4_pFxzbUCQZoYigXoXNJdpXB8I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:12+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
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"v4.0.0" .
}